Targeted delivery and labeling of single living cells
in heterogeneous
cell populations are of great importance to understand the molecular
biology and physiological functions of individual cells. However,
it remains challenging to perfuse fluorescence markers into single
living cells with high spatial and temporal resolution without interfering
neighboring cells. Here, we report a single cell perfusion and fluorescence
labeling strategy based on nanoscale glass nanopipettes. With the
nanoscale tip hole of 100 nm, the use of nanopipettes allows special
perfusion and high-resolution fluorescence labeling of different subcellular
regions in single cells of interest. The dynamic of various fluorescent
probes has been studied to exemplify the feasibility of nanopipette-dependent
targeted delivery. According to experimental results, the cytoplasm
labeling of Sulfo-Cyanine5 and fluorescein isothiocyanate is mainly
based on the Brownian movement due to the dyes themselves and does
not have a targeting ability, while the nucleus labeling of 4′,6-diamidino-2-phenylindole
(DAPI) is originated from the adsorption between DAPI and DNA in the
nucleus. From the finite element simulation, the precise manipulation
of intracellular delivery is realized by controlling the electro-osmotic
flow inside the nanopipettes, and the different delivery modes between
nontargeting dyes and nucleus-targeting dyes were compared, showcasing
the valuable ability of nanopipette-based method for the analysis
of specially defined subcellular regions and the potential applications
for single cell surgery, subcellular manipulation, and gene delivery.